Hosaka Tomooki, Fukabori Taiga, Kojima Haruka, Kubota Kei, Komaba Shinichi
Department of Applied Chemistry, Tokyo University of Science, Shinjuku, Tokyo, 162-8601, Japan.
Elements Strategy Initiative for Catalysts and Batteries (ESICB), Kyoto University, Goryo-Ohara, Nishikyo-ku, Kyoto, 615-8245, Japan.
ChemSusChem. 2021 Feb 18;14(4):1166-1175. doi: 10.1002/cssc.202002628. Epub 2021 Jan 14.
Potassium manganese hexacyanoferrate (KMnHCF) can be used as a positive electrode for potassium-ion batteries because of its high energy density. The effect of particle size and [Fe(CN) ] vacancies on the electrochemical potassium insertion of KMnHCFs was examined through experimental data and theoretical calculations. When nearly stoichiometric KMnHCF was synthesized and tested, smaller particle sizes were found to be important for achieving superior electrochemical performance in terms of capacity and rate capability. However, even in the case of larger particles, introducing a suitable number of anion vacancies enabled KMnHCF to exhibit comparable electrode performance. Electrochemical tests and density functional theory calculations indicated that anion vacancies contribute to the enhancement of K ion diffusion, which realizes good electrochemical performance. Structural design, including crystal vacancies and particle size, is the key to their high performance as a positive electrode.
六氰合铁酸锰钾(KMnHCF)因其高能量密度可作为钾离子电池的正极。通过实验数据和理论计算研究了粒径和[Fe(CN)₆]空位对KMnHCF电化学钾插入的影响。当合成并测试接近化学计量比的KMnHCF时,发现较小的粒径对于在容量和倍率性能方面实现优异的电化学性能很重要。然而,即使在较大颗粒的情况下,引入适量的阴离子空位也能使KMnHCF表现出相当的电极性能。电化学测试和密度泛函理论计算表明,阴离子空位有助于增强K⁺离子扩散,从而实现良好的电化学性能。包括晶体空位和粒径在内的结构设计是其作为正极高性能的关键。